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Volumn 22, Issue 11, 2011, Pages 1205-1211

Organocatalytic enantioselective tandem aldol-cyclization reaction of α-isothiocyanato imides and activated carbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; CINCHONA ALKALOID; IMIDE; ISATIN DERIVATIVE; ISOTHIOCYANIC ACID DERIVATIVE; LACTONE DERIVATIVE; THIOCARBAMIC ACID DERIVATIVE; THIOUREA DERIVATIVE;

EID: 80052607110     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.06.028     Document Type: Article
Times cited : (26)

References (67)
  • 1
    • 0023619369 scopus 로고
    • For selected examples see: (a)
    • For selected examples, see: (a) Evans, D. A.; Weber, A. E. J. Am. Chem. Soc. 1987, 109, 7151;
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7151
    • Evans, D.A.1    Weber, A.E.2
  • 13
    • 77956021172 scopus 로고    scopus 로고
    • For examples of enantioselective tandem Mannich-cyclization reactions, see
    • Vecchione, M. K.; Li, L.; Seidel, D. Chem. Commun. 2010, 4604; For examples of enantioselective tandem Mannich-cyclization reactions, see
    • (2010) Chem. Commun. , pp. 4604
    • Vecchione, M.K.1    Li, L.2    Seidel, D.3
  • 24
    • 77951529935 scopus 로고    scopus 로고
    • For reviews on aldol reactions, see: (a)
    • For reviews on aldol reactions, see: (a) Trost, B. M.; Brindle, C. S. Chem. Soc. Rev. 2010, 39, 1600;
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1600
    • Trost, B.M.1    Brindle, C.S.2
  • 25
    • 11844259698 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim Germany
    • Mahrwald, R. Modern Aldol Reactions; Wiley-VCH: Weinheim, Germany, 2004. pp. 1218-1223;
    • (2004) Modern Aldol Reactions , pp. 1218-1223
    • Mahrwald, R.1
  • 36
    • 33745437193 scopus 로고    scopus 로고
    • The products may be viewed as analogues of spiroindoline phytoalexins. The latter compounds are known to possess potent antimicrobial, antitumor, and oviposition-stimulant biological activities; for examples, see: (a)
    • The products may be viewed as analogues of spiroindoline phytoalexins. The latter compounds are known to possess potent antimicrobial, antitumor, and oviposition-stimulant biological activities; for examples, see: (a) Pedras, M. S. C.; Hossain, M. Org. Biomol. Chem. 2006, 4, 2581;
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 2581
    • Pedras, M.S.C.1    Hossain, M.2
  • 40
    • 38349135345 scopus 로고    scopus 로고
    • For selected reviews on amine thiourea catalysis, see: (a)
    • For selected reviews on amine thiourea catalysis, see: (a) Doyle, A. G.; Jacobsen, E. N. Chem. Rev. 2007, 107, 5713;
    • (2007) Chem. Rev. , vol.107 , pp. 5713
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 43
    • 77950521746 scopus 로고    scopus 로고
    • For selected examples of amine thiourea catalysis, see: (a)
    • For selected examples of amine thiourea catalysis, see: (a) Marcelli, T.; Hiemstra, H. Synthesis 2010, 8, 1229;
    • (2010) Synthesis , vol.8 , pp. 1229
    • Marcelli, T.1    Hiemstra, H.2
  • 54
    • 0022490196 scopus 로고
    • For examples of using the oxazolidinone moiety as an auxilary in organic reactions see: (a)
    • For examples of using the oxazolidinone moiety as an auxilary in organic reactions, see: (a) Evans, D. A.; Weber, A. E. J. Am. Chem. Soc. 1986, 108, 6757;
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6757
    • Evans, D.A.1    Weber, A.E.2
  • 55
    • 0029804421 scopus 로고    scopus 로고
    • and references cited therein
    • Sibi, M. P.; Ji, J. J. Am. Chem. Soc. 1996, 118, 9200. and references cited therein.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9200
    • Sibi, M.P.1    Ji, J.2
  • 56
    • 32644452625 scopus 로고    scopus 로고
    • For examples of using 1,2-diones as electrophiles in organocatalyzed reactions, see: (a)
    • For examples of using 1,2-diones as electrophiles in organocatalyzed reactions, see: (a) Nair, V.; Vellalath, S.; Poonoth, M.; Mohan, R.; Suresh, E. Org. Lett. 2006, 8, 507;
    • (2006) Org. Lett. , vol.8 , pp. 507
    • Nair, V.1    Vellalath, S.2    Poonoth, M.3    Mohan, R.4    Suresh, E.5
  • 64
    • 85030494418 scopus 로고    scopus 로고
    • CCDC deposition number 788041 contains the supplementary crystallographic data for compound 5a. These data can be obtained free of charge from the Cambridge Crystallographic Data center via
    • CCDC deposition number 788041 contains the supplementary crystallographic data for compound 5a. These data can be obtained free of charge from the Cambridge Crystallographic Data center via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.